What are the responsibilities and job description for the Associate, Medical Science Liaison position at Healthcare Businesswomen’s Association?
Job Description Summary
SMLの指示と同意のもと、割り当てられた治療領域と地域における医療専門家エンゲージメント計画を策定します。
Job Description
SMLの指示と同意のもと、割り当てられた治療領域と地域における医療専門家エンゲージメント計画を策定します。
BBOおよび戦略との整合性を確保するために、治療領域における医療専門家エンゲージメント計画を策定します。
SOPなど）を遵守しながら、自発的な臨床試験を設定、実施、追跡します。
Develop the medical expert engagement plan(s) in assigned therapeutic area(s) and local areas under the direction and agreement of Senior MSL Lead.
Develop the medical expert engagement plan in the therapeutic areas to ensure alignment with Senior MSL Lead BBO and Strategies.
Ensure medical insights and medical / scientific intelligence gained in-field informs regional engagement planning, and key issues are addressed with regional colleagues as appropriate.
Set up, conduct and track spontaneous clinical studies while adhering to applicable quality modules and other procedural documents (e.g., SOPs).
MSL活動の実施を推進し、重点バイオシミラー製品の認知度を高め、科学情報を提供します。
SMLの指示と監督の下、結果を追跡してコンプライアンスチームに報告するなど、対象治療領域での助成金活動を運営します。
Drive the implementation of the MSL activities in align with the medical expert engagement plan to increase awareness of the focused biosimilar products and provide scientific information.
Provide the scientific messages to experts in healthcare community via scientific lectures and face-to-face meeting.
Develop a strong network with medical experts nationally and experts in the healthcare community.
Operate grants activities in the targeted therapeutic areas including tracking and reporting the results to compliance team under the direction and supervision of the Senior MSL Lead.
MRなどの他の部門と機能横断的に連携します。
MRに対して製品（特に新発売製品）と疾患に関する科学的トレーニングをサポートします。
Collaborate cross-functionally with other departments such as Medical Representatives.
Support field commercial activities from the scientific perspectives (Providing customers with scientific information upon requests).
Support scientific training about products (especially new launch products) and disease to MRs.
SMLの指示の元に医療監査を準備します。
Ensure all activities and interactions in assigned therapeutic area(s) are conducted with due regard to local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.
Prepare medical audits under the direction of SML.
Ensure vendors are qualified throughout their involvement in the activities.
Partner with the Local Pharmacovigilance team(s) to ensure compliant safety reporting in all affected studies.
Skills Desired
Clinical Research, Clinical Trials, Curiosity, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Patient Care, Physics, Technical Support
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